Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Philippines
FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in the Philippines: 8 establishments
8 establishments in the Philippines are registered with the FDA to make Lens, Spectacle, Non-Custom (Prescription) (product code HQG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Lens, Spectacle, Non-Custom (Prescription)
- Product code
- HQG
- Country
- Philippines
Makers of Lens, Spectacle, Non-Custom (Prescription) in the Philippines
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advance Vision Phils., Inc. | NAIC Cavite, Philippines | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apollo Lens Manufacturing Philippines, Inc. | Naic Cavite, Philippines | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Contour Optik Philippine Inc. | Tanza Cavite, Philippines | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EHS Lens Philippines, Inc Batangas Plant | Tanauan City, Batangas, Philippines | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essilor Manufacturing Philippines Inc. | MARIVELES Bataan, Philippines | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hong Kong Optical Lens Phils. Laboratory Inc. | Quezon City National Capital Region, Philippines | Exporter to the US, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Optodev, Inc. | MAMPLASAN, BINAN Laguna, Philippines | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunnies Inc. | Quezon City, Metro Manila, Philippines | Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.